Senior Associate Regulatory Affairs - Chicago

WeareseekingaRegulatoryAffairsSpecialisttosupportregulatarysubmissions,globalexceptions,labelingreviews,andcomplianceactivitiesforClassII/IIImedicaldevices.Bachelor'sorMaster'sinEngineering,Regulatory,Biomedical,LifesSciences3–7yearsofRegulatoryAffairsexperiencemedinmedicaldevice ...

This is an exciting opportunity to join Conagra Brands as a Manager Regulatory Affairs. In this role, you will support the company in regulatory issues and opportunities. · Provides regulatory leadership and collaborates with Marketing, Sales, R&D... · ...

As a Regulatory Affairs Specialist for Nature's Bakery you will be responsible for all aspects of ingredient on-boarding regulatory documentation regulatory compliance review and 3rd party certification submissions and managing approvals. · ...

The Regulatory Affairs Manager (CMC) position is responsible for authoring, review, preparation and management on-time filing of high-quality regulatory submissions with an emphasis on CMC. · The primary responsibility will include authoring, reviewing and preparing high quality ...

The Regulatory Affairs Manager (CMC) position is responsible for the author, review, · preparation and manage on-time filing of high-quality regulatory submissions · and for post-approval maintenance of regulatory dossiers with an emphasis on CMC. · ...

Work on innovative combination products impacting patients globally. · ...

The Regulatory Affairs Associate will combine regulatory, business, and scientific knowledge to provide support with regulatory submissions, agency responses and internal queries for AbbVie global product portfolio. · ...

About this job: Regulatory Affairs Associate at Collabera in North Chicago, IL. · ...

We are seeking a · Regulatory Affairs Specialist · to support regulatory submissions, · global registrations, · labeling reviews, · and compliance activities for Class II/III medical devices. · ...

Develop global regulatory strategies for medical device products to meet business objectives and collaborates across a matrixed organization to ensure global success of products registration. · Negotiate with regulatory authorities to resolve questions/issues that arise during th ...

This role supports the company in regulatory issues and opportunities. It involves leading projects to ensure regulatory compliance and leveraging opportunities to benefit Conagra Brands. · ...

Reporting to the Senior Director Regulatory Affairs you will support the company in regulatory issues and opportunities. · In this position you will help lead projects programs and/or processes to ensure regulatory compliance and to leverage regulatory opportunities to the benefi ...

Responsible for technical writing of files in accordance with In Vitro Diagnostic medical device Regulation (IVDR) and provides regulatory support for diagnostic product development and commercial diagnostic products. · ...

As a Regulatory Affairs Specialist for Nature's Bakery, you will be responsible for all aspects of ingredient on-boarding, regulatory documentation, regulatory compliance review and third party certification (submissions and managing approvals). You may also play a role in produc ...

We are seeking a Manager to play an integral role in ensuring that Capital One delivers on commitments to our regulators in a timely manner and proactively responds to the changing regulatory landscape. · ...

The Regulatory Affairs Manager (CMC) position is responsible for the author, review, preparation and manage on-time filing of high-quality regulatory submissions and for post-approval maintenance of regulatory dossiers with an emphasis on CMC. · * Assimilate to changing environme ...

The Regulatory Affairs Manager (CMC) position is responsible for authoring, reviewing, preparing high quality regulatory submissions and managing post-approval maintenance of regulatory dossiers with an emphasis on CMC. · Authoring, reviewing and preparing high-quality ANDA, NDA, ...

+Work with a global leader in drug delivery and combination products delivering solutions that improve patient lives. · + · +Develop and execute CMC strategies for combination products · Assess PK/PD impact and support device bridging e.g.vial → autoinjector · ...

+The Regulatory Affairs Manager (CMC) position is responsible for the author review preparation and manage on-time filing of high-quality regulatory submissions and for post-approval maintenance of regulatory dossiers with an emphasis on CMC. · +* Authoring reviewing and preparin ...

This job is with Johnson & Johnson in Mexico City. The Regulatory Affairs Head will manage the coordination and submission of new drug applications to regulatory agencies. ...

The Vice President of Regulatory Affairs will serve as the senior-most regulatory leader responsible for envisioning, developing, and executing the company's global regulatory strategy to support clinical development, product approvals, lifecycle management, and ongoing complianc ...